390-0218

GUDID 00886385022307

Sigmoid Notch Screw

Stryker Trauma SA

Wrist ulna-head prosthesis
Primary Device ID00886385022307
NIH Device Record Key14c85e16-bb54-4629-827a-981a25b9c2de
Commercial Distribution StatusIn Commercial Distribution
Version Model Number390-0218
Catalog Number390-0218
Company DUNS481999654
Company NameStryker Trauma SA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Length20 Millimeter
Length20 Millimeter
Length20 Millimeter
Length20 Millimeter
Length20 Millimeter
Length20 Millimeter
Length20 Millimeter
Length20 Millimeter
Length20 Millimeter
Length20 Millimeter
Length20 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100886385022307 [Primary]

FDA Product Code

KXEPROSTHESIS, WRIST, HEMI-, ULNAR

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-09-24

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